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4N7Y

Crystal structure of 14-3-3zeta in complex with a 8-carbon-linker cyclic peptide derived from ExoS

Summary for 4N7Y
Entry DOI10.2210/pdb4n7y/pdb
Related3CH8 3NKX 4IEA 4IHL 4N7G 4N84
Descriptor14-3-3 protein zeta/delta, Exoenzyme S (3 entities in total)
Functional Keywords14-3-3, adaptor protein, protein-protein interaction, cross-link, signaling protein
Biological sourceHomo sapiens (human)
More
Cellular locationCytoplasm: P63104
Total number of polymer chains4
Total formula weight55811.17
Authors
Bier, D.,Glas, A.,Hahne, G.,Grossmann, T.,Ottmann, C. (deposition date: 2013-10-16, release date: 2014-02-19, Last modification date: 2023-11-15)
Primary citationGlas, A.,Bier, D.,Hahne, G.,Rademacher, C.,Ottmann, C.,Grossmann, T.N.
Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction.
Angew.Chem.Int.Ed.Engl., 53:2489-2493, 2014
Cited by
PubMed Abstract: Bioactive conformations of peptides can be stabilized by macrocyclization, resulting in increased target affinity and activity. Such macrocyclic peptides proved useful as modulators of biological functions, in particular as inhibitors of protein-protein interactions (PPI). However, most peptide-derived PPI inhibitors involve stabilized α-helices, leaving a large number of secondary structures unaddressed. Herein, we present a rational approach towards stabilization of an irregular peptide structure, using hydrophobic cross-links that replace residues crucially involved in target binding. The molecular basis of this interaction was elucidated by X-ray crystallography and isothermal titration calorimetry. The resulting cross-linked peptides inhibit the interaction between human adaptor protein 14-3-3 and virulence factor exoenzyme S. Taking into consideration that irregular peptide structures participate widely in PPIs, this approach provides access to novel peptide-derived inhibitors.
PubMed: 24504455
DOI: 10.1002/anie.201310082
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.16 Å)
Structure validation

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